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G A Fishman

Showing results (191-200 of 224) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|April 17, 1999
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR geneG A Fishman, E M Stone, S Grover, et al.
Ophthalmology|December 1, 1991
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin geneE M Stone, A E Kimura, B E Nichols, et al.
Retina (Philadelphia, Pa.)|January 1, 1987
Magnetic resonance imaging of central nervous system defects in Usher's syndromeL Piazza, G A Fishman, R D Kaplan, et al.
Human Mutation|December 19, 2001
Novel frameshift mutations in CRX associated with Leber congenital amaurosisC Rivolta, N E Peck, A B Fulton, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosaG A Fishman, K Vandenburgh, E M Stone, et al.
Ophthalmology|February 1, 1997
Serine-27-phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophyG A Fishman, E M Stone, K R Alexander, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1984
Birdshot retinochoroidopathyD J Fuerst, H H Tessler, G A Fishman, et al.
Retina (Philadelphia, Pa.)|January 1, 1987
Antiphospholipid antibodies associated with retinal vascular diseaseJ S Pulido, L M Ward, G A Fishman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Relationship between difficulty in performing daily activities and clinical measures of visual function in patients with retinitis pigmentosaJ P Szlyk, G A Fishman, K R Alexander, et al.
Transplantation|September 12, 1998
Night blindness secondary to vitamin A deficiency in a patient with bile duct strictures after liver transplantationS Urayama, T W Lissoos, G A Fishman, et al.
Pageof 23

Showing results (191-200 of 224) with videos related to

Sort By:
Pageof 23
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 17, 1999
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR geneG A Fishman, E M Stone, S Grover, et al.
Ophthalmology|December 1, 1991
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin geneE M Stone, A E Kimura, B E Nichols, et al.
Retina (Philadelphia, Pa.)|January 1, 1987
Magnetic resonance imaging of central nervous system defects in Usher's syndromeL Piazza, G A Fishman, R D Kaplan, et al.
Human Mutation|December 19, 2001
Novel frameshift mutations in CRX associated with Leber congenital amaurosisC Rivolta, N E Peck, A B Fulton, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosaG A Fishman, K Vandenburgh, E M Stone, et al.
Ophthalmology|February 1, 1997
Serine-27-phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophyG A Fishman, E M Stone, K R Alexander, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1984
Birdshot retinochoroidopathyD J Fuerst, H H Tessler, G A Fishman, et al.
Retina (Philadelphia, Pa.)|January 1, 1987
Antiphospholipid antibodies associated with retinal vascular diseaseJ S Pulido, L M Ward, G A Fishman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Relationship between difficulty in performing daily activities and clinical measures of visual function in patients with retinitis pigmentosaJ P Szlyk, G A Fishman, K R Alexander, et al.
Transplantation|September 12, 1998
Night blindness secondary to vitamin A deficiency in a patient with bile duct strictures after liver transplantationS Urayama, T W Lissoos, G A Fishman, et al.
Pageof 23